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胶原纤维运动学的改变决定了加载过程中局部韧带损伤的起始。

Altered collagen fiber kinematics define the onset of localized ligament damage during loading.

作者信息

Quinn Kyle P, Winkelstein Beth A

机构信息

Dept. of Bioengineering, Univ. of Pennsylvania, 240 Skirkanich Hall, 210 S. 33rd St., Philadelphia, PA 19104-6321, USA.

出版信息

J Appl Physiol (1985). 2008 Dec;105(6):1881-8. doi: 10.1152/japplphysiol.90792.2008. Epub 2008 Oct 9.

Abstract

Detecting the initiation of mechanical injury to biological tissue, and not just its ultimate failure, is critical to a sensitive and specific characterization of tissue tolerance, development of quantitative relationships between macro- and microstructural tissue responses, and appropriate interpretation of physiological responses to loading. We have developed a novel methodological approach to detect the onset and spatial location of structural damage in collagenous soft tissue, before its visible rupture, via identification of atypical regional collagen fiber kinematics during loading. Our methods utilize high-speed quantitative polarized light imaging to identify the onset of tissue damage in ligament regions where mean collagen fiber rotation significantly deviates from its behavior during noninjurious loading. This technique was validated by its ability to predict the location of visible rupture (P = 0.0009). This fiber rotation-based metric of damage identifies potential facet capsular ligament injury beginning well before rupture, at 51 +/- 12% of the displacement required to produce tissue failure. Although traditional macroscale strain metrics fail to identify the location of microstructural damage, initial injury detection determined by altered fiber rotation was significantly correlated (R = 0.757, P = 0.049) with tissue yield (defined by a decrease in stiffness), supporting the capabilities of this method. Damaged regions exhibited higher variance in fiber direction than undamaged regions (P = 0.0412).

摘要

检测生物组织机械损伤的起始,而不仅仅是其最终失效,对于敏感且特异性地表征组织耐受性、建立宏观和微观结构组织反应之间的定量关系以及正确解释对负荷的生理反应至关重要。我们开发了一种新颖的方法,通过识别加载过程中非典型的局部胶原纤维运动学,在胶原软组织可见破裂之前检测其结构损伤的起始和空间位置。我们的方法利用高速定量偏振光成像来识别韧带区域中组织损伤的起始,在该区域平均胶原纤维旋转明显偏离其在非损伤性加载期间的行为。该技术通过其预测可见破裂位置的能力得到验证(P = 0.0009)。这种基于纤维旋转的损伤度量能够在破裂前很久就识别潜在的关节囊韧带损伤,此时的位移为产生组织失效所需位移的51 +/- 12%。尽管传统的宏观应变度量无法识别微观结构损伤的位置,但由纤维旋转改变所确定的初始损伤检测与组织屈服(由刚度降低定义)显著相关(R = 0.757,P = 0.049),这支持了该方法的能力。受损区域的纤维方向比未受损区域表现出更高的方差(P = 0.0412)。

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